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Journal Abstract Search

356 related items for PubMed ID: 21511817

  • 21. [Mutational analysis of MYO1E in children with sporadic steroid-resistant nephrotic syndrome in Chinese Han ethnic group].
    Zhao F, Yu Z, Yang Y, Nie X, Huang J, Wang C, Xia G, Chen G.
    Zhonghua Er Ke Za Zhi; 2014 Jul; 52(7):488-93. PubMed ID: 25224051
    [Abstract] [Full Text] [Related]

  • 22. TRPC6 and FSGS: the latest TRP channelopathy.
    Mukerji N, Damodaran TV, Winn MP.
    Biochim Biophys Acta; 2007 Aug; 1772(8):859-68. PubMed ID: 17459670
    [Abstract] [Full Text] [Related]

  • 23. Clinical utility of genetic testing in children and adults with steroid-resistant nephrotic syndrome.
    Santín S, Bullich G, Tazón-Vega B, García-Maset R, Giménez I, Silva I, Ruíz P, Ballarín J, Torra R, Ars E.
    Clin J Am Soc Nephrol; 2011 May; 6(5):1139-48. PubMed ID: 21415313
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  • 24. NPHS2 mutations in sporadic steroid-resistant nephrotic syndrome in Japanese children.
    Maruyama K, Iijima K, Ikeda M, Kitamura A, Tsukaguchi H, Yoshiya K, Hoshii S, Wada N, Uemura O, Satomura K, Honda M, Yoshikawa N.
    Pediatr Nephrol; 2003 May; 18(5):412-6. PubMed ID: 12687458
    [Abstract] [Full Text] [Related]

  • 25. Report of novel genetic variation in NPHS2 gene associated with idiopathic nephrotic syndrome in South Indian children.
    Dhandapani MC, Venkatesan V, Rengaswamy NB, Gowrishankar K, Ekambaram S, Sengutavan P, Perumal V.
    Clin Exp Nephrol; 2017 Feb; 21(1):127-133. PubMed ID: 26820844
    [Abstract] [Full Text] [Related]

  • 26. Genetic variations of the NR3C1 gene in children with sporadic nephrotic syndrome.
    Ye J, Yu Z, Ding J, Chen Y, Huang J, Yao Y, Xiao H, Yang J, Shen Y, Meng Q.
    Biochem Biophys Res Commun; 2006 Sep 22; 348(2):507-13. PubMed ID: 16890204
    [Abstract] [Full Text] [Related]

  • 27. Steroid-resistant idiopathic childhood nephrosis: overdiagnosed and undertreated.
    Ehrich JH, Geerlings C, Zivicnjak M, Franke D, Geerlings H, Gellermann J.
    Nephrol Dial Transplant; 2007 Aug 22; 22(8):2183-93. PubMed ID: 17504846
    [Abstract] [Full Text] [Related]

  • 28. NPHS2 gene in steroid-resistant nephrotic syndrome: prevalence, clinical course, and mutational spectrum in South-West Iranian children.
    Basiratnia M, Yavarian M, Torabinezhad S, Erjaee A.
    Iran J Kidney Dis; 2013 Sep 22; 7(5):357-62. PubMed ID: 24072147
    [Abstract] [Full Text] [Related]

  • 29. Cyclosporine in patients with steroid-resistant nephrotic syndrome: an open-label, nonrandomized, retrospective study.
    Ghiggeri GM, Catarsi P, Scolari F, Caridi G, Bertelli R, Carrea A, Sanna-Cherchi S, Emma F, Allegri L, Cancarini G, Rizzoni GF, Perfumo F.
    Clin Ther; 2004 Sep 22; 26(9):1411-8. PubMed ID: 15531003
    [Abstract] [Full Text] [Related]

  • 30. A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from Pakistan.
    Abid A, Khaliq S, Shahid S, Lanewala A, Mubarak M, Hashmi S, Kazi J, Masood T, Hafeez F, Naqvi SA, Rizvi SA, Mehdi SQ.
    Gene; 2012 Jul 10; 502(2):133-7. PubMed ID: 22565185
    [Abstract] [Full Text] [Related]

  • 31. Wilms' tumor suppressor gene mutations in girls with sporadic isolated steroid-resistant nephrotic syndrome.
    Yang YH, Zhao F, Feng DN, Wang JJ, Wang CF, Huang J, Nie XJ, Xia GZ, Chen GM, Yu ZH.
    Genet Mol Res; 2013 Dec 04; 12(4):6184-91. PubMed ID: 24338413
    [Abstract] [Full Text] [Related]

  • 32. Clinical characteristics and WT1 genetic analysis of patients with steroid resistant nephrotic syndrome accompanied with genitourinary malformations.
    Li JG, Zhao D, Ding J, Xiao HJ, Guan N, Fan QF, Zhang HW.
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2007 Dec 04; 32(6):949-57. PubMed ID: 18182709
    [Abstract] [Full Text] [Related]

  • 33. Mutations in the Wilms' tumor 1 gene cause isolated steroid resistant nephrotic syndrome and occur in exons 8 and 9.
    Mucha B, Ozaltin F, Hinkes BG, Hasselbacher K, Ruf RG, Schultheiss M, Hangan D, Hoskins BE, Everding AS, Bogdanovic R, Seeman T, Hoppe B, Hildebrandt F, Members of the APN Study Group.
    Pediatr Res; 2006 Feb 04; 59(2):325-31. PubMed ID: 16439601
    [Abstract] [Full Text] [Related]

  • 34. Dominant PAX2 mutations may cause steroid-resistant nephrotic syndrome and FSGS in children.
    Vivante A, Chacham OS, Shril S, Schreiber R, Mane SM, Pode-Shakked B, Soliman NA, Koneth I, Schiffer M, Anikster Y, Hildebrandt F.
    Pediatr Nephrol; 2019 Sep 04; 34(9):1607-1613. PubMed ID: 31001663
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  • 35. A Systematic Analysis of Major Susceptible Genes in Childhood-onset Steroid-resistant Nephrotic Syndrome.
    Li Y, He Q, Wang Y, Dang X, Wu X, Li X, Shuai L, Yi Z.
    Ann Clin Lab Sci; 2019 May 04; 49(3):330-337. PubMed ID: 31308032
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  • 36. Pattern of steroid resistant nephrotic syndrome in children living in the kingdom of Saudi Arabia: a single center study.
    Kari JA, Halawani M, Mokhtar G, Jalalah SM, Anshasi W.
    Saudi J Kidney Dis Transpl; 2009 Sep 04; 20(5):854-7. PubMed ID: 19736491
    [Abstract] [Full Text] [Related]

  • 37. [Four cases of nephrotic syndrome with TRPC6 gene variations and literature review].
    Sun LW, Sun L, Wang P, Kang YL, Wu Y, Zhu GH, Huang WY.
    Zhonghua Er Ke Za Zhi; 2021 Mar 02; 59(3):223-227. PubMed ID: 33657698
    [Abstract] [Full Text] [Related]

  • 38. TRPC6 and NPHS2 gene variants in adult patients with steroid-resistant nephrotic syndrome in North-West of Iran.
    Zununi Vahed S, Moghaddas Sani H, Haghi M, Mohajel Shoja M, Ardalan M.
    Mol Biol Rep; 2019 Dec 02; 46(6):6339-6344. PubMed ID: 31529341
    [Abstract] [Full Text] [Related]

  • 39. CD2AP mutations are associated with sporadic nephrotic syndrome and focal segmental glomerulosclerosis (FSGS).
    Gigante M, Pontrelli P, Montemurno E, Roca L, Aucella F, Penza R, Caridi G, Ranieri E, Ghiggeri GM, Gesualdo L.
    Nephrol Dial Transplant; 2009 Jun 02; 24(6):1858-64. PubMed ID: 19131354
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  • 40. MDR-1 gene polymorphisms in steroid-responsive versus steroid-resistant nephrotic syndrome in children.
    Jafar T, Prasad N, Agarwal V, Mahdi A, Gupta A, Sharma RK, Negi MP, Agrawal S.
    Nephrol Dial Transplant; 2011 Dec 02; 26(12):3968-74. PubMed ID: 21460357
    [Abstract] [Full Text] [Related]

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